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Autosomal dominant spastic paraplegia type 37

ORPHA:171612· ICD-10 G11.4

Definition

A pure form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive spastic gait, extensor plantar responses, brisk tendon reflexes in arms and legs, decreased vibration sense at ankles and urinary dysfunction. Ankle clonus is also reported in some patients.

Prevalence
<1 / 1 000 000
Inheritance
Autosomal dominant
Age of onset
All ages